Liquorice root extract and isoliquiritigenin attenuate high-fat diet-induced hepatic steatosis and damage in rats by regulating AMPK.

IF 4.7 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-08-01 Epub Date: 2022-09-19 DOI:10.1080/13813455.2022.2102654
Mohammed Abdo Yahya, Ghedeir M Alshammari, Magdi A Osman, Laila Naif Al-Harbi, Abu ElGasim A Yagoub, Sahar Abdulaziz AlSedairy
{"title":"Liquorice root extract and isoliquiritigenin attenuate high-fat diet-induced hepatic steatosis and damage in rats by regulating AMPK.","authors":"Mohammed Abdo Yahya, Ghedeir M Alshammari, Magdi A Osman, Laila Naif Al-Harbi, Abu ElGasim A Yagoub, Sahar Abdulaziz AlSedairy","doi":"10.1080/13813455.2022.2102654","DOIUrl":null,"url":null,"abstract":"<p><p><b>Objective:</b> This study compared the ability of Liquorice roots aqueous extract (LRE) and its ingredient, isoliquiritigenin (ISL), in alleviating high-fat diet (HFD)-induced hepatic steatosis and examined if this effect involves activation of AMPK.<b>Materials and methods:</b> Control or HFD-fed rats were treated with the vehicle, LRE (200 mg/kg), or ISL (30 mg/kg) for 8 weeks orally.<b>Results:</b> ISL and LRE reduced HFD-induced hyperglycaemia, improved liver structure, lowered serum and hepatic lipids, and attenuated hepatic oxidative stress and inflammation. In the control and HFD-fed rats, ISL and LRE significantly stimulated the muscular and hepatic mRNA and protein levels of AMPK, improved oral glucose tolerance, reduced hepatic mRNA levels of SREBP1/2, and upregulated hepatic levels of PPARα and Bcl2. These effects were comparable for ISL and LRE and were prevented by co-administration of compound C, an AMPK inhibitor.<b>Discussion and conclusion:</b> ISL and LRE provide an effective theory to alleviate hepatic steatosis through activating AMPK.</p>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":" ","pages":"385-400"},"PeriodicalIF":4.7000,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/13813455.2022.2102654","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2022/9/19 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
引用次数: 0

Abstract

Objective: This study compared the ability of Liquorice roots aqueous extract (LRE) and its ingredient, isoliquiritigenin (ISL), in alleviating high-fat diet (HFD)-induced hepatic steatosis and examined if this effect involves activation of AMPK.Materials and methods: Control or HFD-fed rats were treated with the vehicle, LRE (200 mg/kg), or ISL (30 mg/kg) for 8 weeks orally.Results: ISL and LRE reduced HFD-induced hyperglycaemia, improved liver structure, lowered serum and hepatic lipids, and attenuated hepatic oxidative stress and inflammation. In the control and HFD-fed rats, ISL and LRE significantly stimulated the muscular and hepatic mRNA and protein levels of AMPK, improved oral glucose tolerance, reduced hepatic mRNA levels of SREBP1/2, and upregulated hepatic levels of PPARα and Bcl2. These effects were comparable for ISL and LRE and were prevented by co-administration of compound C, an AMPK inhibitor.Discussion and conclusion: ISL and LRE provide an effective theory to alleviate hepatic steatosis through activating AMPK.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
甘草根提取物和甘草次甙元通过调节 AMPK 减轻高脂饮食引起的大鼠肝脏脂肪变性和损伤
研究目的本研究比较了甘草根水提取物(LRE)及其成分ISL(isiquiritigenin)在缓解高脂饮食(HFD)诱导的肝脏脂肪变性方面的能力,并考察了这种作用是否涉及AMPK的激活:对照组或高脂饮食喂养的大鼠口服载体、LRE(200 毫克/千克)或 ISL(30 毫克/千克)治疗 8 周:结果:ISL和LRE降低了HFD诱导的高血糖,改善了肝脏结构,降低了血清和肝脏脂质,减轻了肝脏氧化应激和炎症反应。在对照组和高氟日粮喂养的大鼠中,ISL 和 LRE 能显著刺激肌肉和肝脏中 AMPK 的 mRNA 和蛋白质水平,改善口服葡萄糖耐量,降低肝脏中 SREBP1/2 的 mRNA 水平,上调肝脏中 PPARα 和 Bcl2 的水平。这些效应在 ISL 和 LRE 中具有可比性,同时服用 AMPK 抑制剂化合物 C 可防止这些效应:ISL和LRE为通过激活AMPK缓解肝脏脂肪变性提供了一种有效的理论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
期刊介绍: ACS Applied Bio Materials is an interdisciplinary journal publishing original research covering all aspects of biomaterials and biointerfaces including and beyond the traditional biosensing, biomedical and therapeutic applications. The journal is devoted to reports of new and original experimental and theoretical research of an applied nature that integrates knowledge in the areas of materials, engineering, physics, bioscience, and chemistry into important bio applications. The journal is specifically interested in work that addresses the relationship between structure and function and assesses the stability and degradation of materials under relevant environmental and biological conditions.
期刊最新文献
Dual Antibacterial and Anticancer Functionality of Self-Assembled Dipeptide-Capped Silver Nanoparticles: Molecular Insights into Protein-Nanoparticle Interactions. Simultaneous Cross-Linking and Nanoparticle Anchoring by Dialdehyde Cellulose in Injectable Composite Chitosan/Polypyrrole Hydrogels. Biocompatibility of Additively Manufactured Fe-AZ31 Biodegradable Composites for Craniofacial Implant Applications. Decellularized Dermis ECM-Based Melanoma-on-a-Chip Model with Integrated Lymphatic and Vascular Networks for High-Throughput Drug Testing. Physically Cross-Linked Hydrogels Based on Poly(vinyl alcohol) and Gelatin for Independent Modulation of Mechanical Cues in Cell Adhesion Studies.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1